ArticleCureus2025
Innovation in Onychomycosis Treatment Through Creative Compounding.
Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
0 citing papers in PubMed.
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Corrections and comments
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Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Onychomycosis is a common fungal nail infection, often presenting with nail discoloration, thickening, and brittleness. Despite the availability of oral and topical antifungal agents, recurrence rates remain high, and systemic therapies can pose risks such as hepatotoxicity and drug interactions. This case report describes an innovative treatment approach using a compounded topical preparation made by combining a crushed 250 mg oral terbinafine tablet with an over-the-counter 1% tolnaftate nail lacquer. A healthy 28-year-old female presented with diffuse toenail onychomycosis affecting all digits. After declining oral therapy, she initiated daily application of the compounded lacquer for 10 months. Weekly complete removal and reapplication were performed, and the vial was shaken before each use to maintain a homogenous mixture. The patient documented progress photographically and reported high satisfaction with a significant improvement in nail appearance. No adverse effects were noted. This topical use of pulverized terbinafine takes advantage of the drug's favorable molecular profile for nail penetration, offering targeted treatment with minimal systemic absorption. The estimated daily delivery of terbinafine per nail was approximately 0.4 mg, a potentially therapeutic dose when applied consistently over time. This case supports the potential of creative compounding in expanding safe and patient-friendly treatment options for onychomycosis, especially for individuals who are unable or unwilling to take oral antifungals. Further studies are needed to evaluate the efficacy, pharmacokinetics, and broader applicability of this approach.
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